INF2(redirected from MGC13251)
INF2A gene on chromosome 14q32.33 that encodes a diaphanous formin, which in mice plays a role in polymerisation and depolymerisation of actin filaments.
INF2 mutations are associated with focal segmental glomerulosclerosis type 5, as well as some cases of Charcot-Tooth-Marie neuropathy.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.